Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,488 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,488 in last 12 months

Showing 2028120300 of 28,127 recalls

Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Product Usage: Unloader Custom is an external knee Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Papoose Infant Spine Immobilizer Item # Item Description: PA-100 Papoose...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: NecLoc Extrication Collar Product Usage: Necloc collars are applied to...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Covidien Medical Products (Shanghai) Manufacturing L.L.C.

Recalled Item: Short Percutaneous Antenna with Thermosphere" Technology Standard...

The Issue: Medtronic is voluntarily recalling specific item codes and production lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Medtronic Inc.

Recalled Item: Reveal LINQ insertable Cardiac Monitor Recalled by Medtronic Inc. Due to...

The Issue: Medtronic has identified an issue with the sensitivity of an algorithm used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator Recalled by...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i oxygenators Custom tubing packs for the oxygenator Recalled by...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number:...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Custom Tubing Packs Custom tubing pack for oxygenators Recalled by Maquet...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Mako Surgical Corporation

Recalled Item: RESTORIS PST RIO Offset Shell Impactor For use by orthopedic Recalled by...

The Issue: Potential disassociation of the orientation pin.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2016· Pentax Medical Company

Recalled Item: Video Duodenoscope Recalled by Pentax Medical Company Due to Pentax Medical...

The Issue: Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing